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PL2547679T3 - 2,3-dihydro-1H-inden-1-yl-2,7-diazaspiro [3.5] nonane derivatives and their use as ghrelin receptor antagonists or inverse agonists - Google Patents

2,3-dihydro-1H-inden-1-yl-2,7-diazaspiro [3.5] nonane derivatives and their use as ghrelin receptor antagonists or inverse agonists

Info

Publication number
PL2547679T3
PL2547679T3 PL11713083T PL11713083T PL2547679T3 PL 2547679 T3 PL2547679 T3 PL 2547679T3 PL 11713083 T PL11713083 T PL 11713083T PL 11713083 T PL11713083 T PL 11713083T PL 2547679 T3 PL2547679 T3 PL 2547679T3
Authority
PL
Poland
Prior art keywords
diazaspiro
inden
dihydro
receptor antagonists
inverse agonists
Prior art date
Application number
PL11713083T
Other languages
Polish (pl)
Inventor
Samit Kumar Bhattacharya
Kimberly O'keefe Cameron
Dilinie Prasadhini Fernando
Daniel Wei-Shung Kung
Allyn Timothy Londregan
Kim Francis Mcclure
Suvi Tuula Marjukka Simila
Original Assignee
Pfizer
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Pfizer filed Critical Pfizer
Publication of PL2547679T3 publication Critical patent/PL2547679T3/en

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/10Spiro-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/47Quinolines; Isoquinolines
    • A61K31/4747Quinolines; Isoquinolines spiro-condensed
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/4965Non-condensed pyrazines
    • A61K31/497Non-condensed pyrazines containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/53Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/04Anorexiants; Antiobesity agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/04Ortho-condensed systems
    • C07D491/056Ortho-condensed systems with two or more oxygen atoms as ring hetero atoms in the oxygen-containing ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D513/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D519/00Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Engineering & Computer Science (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Diabetes (AREA)
  • Obesity (AREA)
  • Hematology (AREA)
  • Endocrinology (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Child & Adolescent Psychology (AREA)
  • Emergency Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
PL11713083T 2010-03-19 2011-03-11 2,3-dihydro-1H-inden-1-yl-2,7-diazaspiro [3.5] nonane derivatives and their use as ghrelin receptor antagonists or inverse agonists PL2547679T3 (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US31552210P 2010-03-19 2010-03-19
US201161444401P 2011-02-18 2011-02-18
PCT/IB2011/051035 WO2011114271A1 (en) 2010-03-19 2011-03-11 2,3 dihydro-1h-inden-1-yl- 2,7-diazaspiro [3.6] nonane derivatives and their use as antagonists or inverse agonists of the ghrelin receptor
EP11713083.1A EP2547679B1 (en) 2010-03-19 2011-03-11 2,3 dihydro-1h-inden-1-yl-2,7-diazaspiro[3.6]nonane derivatives and their use as antagonists or inverse agonists of the ghrelin receptor

Publications (1)

Publication Number Publication Date
PL2547679T3 true PL2547679T3 (en) 2016-02-29

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PL11713083T PL2547679T3 (en) 2010-03-19 2011-03-11 2,3-dihydro-1H-inden-1-yl-2,7-diazaspiro [3.5] nonane derivatives and their use as ghrelin receptor antagonists or inverse agonists

Country Status (27)

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US (2) US8609680B2 (en)
EP (1) EP2547679B1 (en)
JP (1) JP5496409B2 (en)
KR (1) KR101455917B1 (en)
CN (1) CN102939290B (en)
AR (1) AR080688A1 (en)
AU (1) AU2011228699B2 (en)
BR (1) BR112012023664B1 (en)
CA (1) CA2792234C (en)
CY (1) CY1118721T1 (en)
DK (1) DK2547679T3 (en)
ES (1) ES2557895T3 (en)
HK (1) HK1182094A1 (en)
HR (1) HRP20151232T1 (en)
HU (1) HUE025774T2 (en)
IL (1) IL221952A (en)
ME (1) ME02330B (en)
MX (1) MX2012010772A (en)
PH (1) PH12012501800A1 (en)
PL (1) PL2547679T3 (en)
PT (1) PT2547679E (en)
RS (1) RS54383B1 (en)
RU (1) RU2524341C2 (en)
SG (1) SG183812A1 (en)
SI (1) SI2547679T1 (en)
TW (1) TWI410423B (en)
WO (1) WO2011114271A1 (en)

Families Citing this family (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101708989B1 (en) * 2012-06-04 2017-02-21 화이자 인코포레이티드 Use of ghrelin receptor inverse agonists or antagonists for treating sleep disorders
EP2861566B1 (en) * 2012-06-13 2016-12-21 F. Hoffmann-La Roche AG New diazaspirocycloalkane and azaspirocycloalkane
SI2900669T1 (en) 2012-09-25 2019-12-31 F. Hoffmann-La Roche Ag Hexahydropyrrolo(3,4-c)pyrrole derivatives and related compounds as autotaxin (atx) inhibitors and as inhibitors of the lysophosphatidic acid (lpa) production for treating e.g. renal diseases
AR095079A1 (en) 2013-03-12 2015-09-16 Hoffmann La Roche DERIVATIVES OF OCTAHIDRO-PIRROLO [3,4-C] -PIRROL AND PIRIDINA-FENILO
US8652527B1 (en) 2013-03-13 2014-02-18 Upsher-Smith Laboratories, Inc Extended-release topiramate capsules
US9101545B2 (en) 2013-03-15 2015-08-11 Upsher-Smith Laboratories, Inc. Extended-release topiramate capsules
RS56776B1 (en) 2013-11-26 2018-04-30 Hoffmann La Roche Octahydro-cyclobuta [1,2-c;3,4-c']dipyrrole derivatives as autotaxin inhibitors
SI3119782T1 (en) * 2014-03-17 2018-06-29 reMYND NV Bio-Incubator 2,7-diazaspiro(3.5)nonane compounds
MX370659B (en) 2014-03-26 2019-12-19 Hoffmann La Roche Bicyclic compounds as autotaxin (atx) and lysophosphatidic acid (lpa) production inhibitors.
CA2935612A1 (en) 2014-03-26 2015-10-01 F. Hoffmann-La Roche Ag Condensed [1,4]diazepine compounds as autotaxin (atx) and lysophosphatidic acid (lpa) production inhibitors
CN104610143A (en) * 2015-02-12 2015-05-13 佛山市赛维斯医药科技有限公司 Glucokinase activator containing nitroquinoline structure and application of glucokinase activator
MA41898A (en) 2015-04-10 2018-02-13 Hoffmann La Roche BICYCLIC QUINAZOLINONE DERIVATIVES
PE20180479A1 (en) 2015-09-04 2018-03-07 Hoffmann La Roche NEW DERIVATIVES OF PHENOXYMETHYL
RU2724899C2 (en) 2015-09-24 2020-06-26 Ф. Хоффманн-Ля Рош Аг New bicyclic compounds as dual inhibitors of atx/ca
MA42919A (en) 2015-09-24 2018-08-01 Hoffmann La Roche BICYCLIC COMPOUNDS USED AS ATX INHIBITORS
CR20180143A (en) 2015-09-24 2018-05-03 Hoffmann La Roche NEW BICYCLE COMPOUNDS AS DUAL INHIBITORS OF ATX / CA
KR20180054830A (en) 2015-09-24 2018-05-24 에프. 호프만-라 로슈 아게 Bifunctional compounds as autotaxine (ATX) inhibitors
KR20180096406A (en) 2017-02-21 2018-08-29 엘지전자 주식회사 refrigerator
CA3053329A1 (en) 2017-03-16 2018-09-20 F. Hoffmann-La Roche Ag Heterocyclic compounds useful as dual atx/ca inhibitors
WO2018167113A1 (en) 2017-03-16 2018-09-20 F. Hoffmann-La Roche Ag New bicyclic compounds as atx inhibitors
CN111225896B (en) 2017-07-28 2024-03-26 凯莫森特里克斯股份有限公司 Immunomodulatory compounds
CN108588215A (en) * 2018-05-03 2018-09-28 成都中创清科医学检验所有限公司 A kind of primer and its detection method for detecting the relevant SNP site of familial hypercholesterolemia neurological susceptibility
CN109970631A (en) * 2019-03-26 2019-07-05 上海吉奉生物科技有限公司 A kind of synthetic method of the iodo- 2- pyridylacetic acid of 5-
CN110256349B (en) * 2019-04-23 2020-09-08 苏州大学 Polysubstituted pyrazole and preparation method thereof
CN110172062B (en) * 2019-06-21 2022-01-07 南京药石科技股份有限公司 Synthesis method of monofluoro spiro compound and intermediate thereof
MX2023006186A (en) 2020-11-27 2023-08-07 Shenzhen Salubris Pharm Co Ltd Benzimidazole derivative and preparation method therefor and medical use thereof.
US12186306B2 (en) 2020-12-10 2025-01-07 Vertex Pharmaceuticals Incorporated Methods of treatment for cystic fibrosis
KR20220001745U (en) 2021-01-06 2022-07-13 성보라 Auxiliary cover for rear protection of automobile seat

Family Cites Families (31)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
LT3595B (en) 1993-01-21 1995-12-27 Schering Corp Spirocycloalkyl-substituted azetidinones useful as hypocholesterolemic agents
NZ527364A (en) 2001-02-28 2004-12-24 Merck & Co Inc Acylated piperidine derivatives as melanocortin-4 receptor agonists
CA2460340C (en) 2001-09-21 2011-02-15 Schering Corporation Methods and therapeutic combinations for the treatment of xanthoma using sterol absorption inhibitors
KR20040095239A (en) 2002-02-27 2004-11-12 화이자 프로덕츠 인코포레이티드 Acc inhibitors
SE0302811D0 (en) 2003-10-23 2003-10-23 Astrazeneca Ab Novel compounds
AU2005247684B2 (en) 2004-05-12 2008-10-23 Pfizer Products Inc. Proline derivatives and their use as dipeptidyl peptidase IV inhibitors
UA84208C2 (en) 2004-05-25 2008-09-25 Пфайзер Продактс Инк. Tetraazabenzo(e)azulene derivatives and analogs thereof
PA8660701A1 (en) 2005-02-04 2006-09-22 Pfizer Prod Inc SMALL AGONISTS AND THEIR USES
GB0514018D0 (en) * 2005-07-07 2005-08-17 Ionix Pharmaceuticals Ltd Chemical compounds
US8168783B2 (en) 2005-11-18 2012-05-01 Ono Pharmaceutical Co., Ltd. Chemokine receptor antagonists and use thereof
EP1962835A2 (en) 2005-12-21 2008-09-03 Schering Corporation Treatment of nonalcoholic fatty liver disease using cholesterol lowering agents and/or h3 receptor antagonist/inverse agonist
PT2463283E (en) 2006-04-20 2014-08-27 Pfizer Prod Inc Fused phenyl amido heterocyclic compounds for the prevention and treatment of glucokinase-mediated diseases
JP2010503675A (en) * 2006-09-15 2010-02-04 シェーリング コーポレイション Spiro-condensed azetidine derivatives useful for the treatment of pain, diabetes and disorders of lipid metabolism
CN101528227A (en) * 2006-09-15 2009-09-09 先灵公司 Azetidinone derivatives and methods of use thereof
JP2010511035A (en) 2006-11-29 2010-04-08 ファイザー・プロダクツ・インク Spiroketone acetyl CoA carboxylase inhibitor
US20090036425A1 (en) 2007-08-02 2009-02-05 Pfizer Inc Substituted bicyclolactam compounds
EP2297163B1 (en) 2008-05-28 2015-07-08 Pfizer Inc. Pyrazolospiroketone acetyl-CoA carboxylase inhibitors
WO2009144555A1 (en) 2008-05-28 2009-12-03 Pfizer Inc. Pyrazolospiroketone acetyl-coa carboxylase inhibitors
JPWO2009154132A1 (en) * 2008-06-19 2011-12-01 Msd株式会社 Spirodiamine-diarylketoxime derivatives
EP2318370A1 (en) 2008-07-29 2011-05-11 Pfizer Inc. Fluorinated heteroaryls
KR101338540B1 (en) 2008-08-28 2013-12-06 화이자 인코포레이티드 Dioxa-bicyclo[3.2.1]octane-2,3,4-triol derivatives
TW201038580A (en) 2009-02-02 2010-11-01 Pfizer 4-amino-5-oxo-7,8-dihydropyrimido[5,4-f][1,4]oxazepin-6(5H)-yl)phenyl derivatives
AP3179A (en) 2009-03-11 2015-03-31 Pfizer Benzofuranyl derivatives used as glucokinase inhibitors
CA2754685A1 (en) 2009-03-11 2010-09-16 Pfizer Inc. Substituted indazole amides
WO2010106457A2 (en) 2009-03-20 2010-09-23 Pfizer Inc. 3-oxa-7-azabicyclo[3.3.1]nonanes
TW201038572A (en) * 2009-03-25 2010-11-01 Gruenenthal Gmbh Substituted spiro-amide compounds
US20120052130A1 (en) 2009-05-08 2012-03-01 Pfizer Inc. Gpr 119 modulators
EP2427450A1 (en) 2009-05-08 2012-03-14 Pfizer Inc. Gpr 119 modulators
NZ596467A (en) 2009-06-05 2014-01-31 Pfizer L- ( piperidin-4-yl) -pyrazole derivatives as gpr 119 modulators
US20120083476A1 (en) * 2009-06-05 2012-04-05 Janssen Pharmaceutica Nv Heteroaryl-substituted spirocyclic diamine urea modulators of fatty acid amide hydrolase
WO2011005611A1 (en) 2009-07-09 2011-01-13 Merck Sharp & Dohme Corp. Neuromedin u receptor agonists and uses thereof

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Publication number Publication date
US8609680B2 (en) 2013-12-17
RU2012137489A (en) 2014-04-27
CN102939290B (en) 2015-09-16
MX2012010772A (en) 2012-11-06
WO2011114271A1 (en) 2011-09-22
EP2547679A1 (en) 2013-01-23
ES2557895T3 (en) 2016-01-29
IL221952A (en) 2016-02-29
AU2011228699A1 (en) 2012-09-20
RS54383B1 (en) 2016-04-28
EP2547679B1 (en) 2015-11-04
PT2547679E (en) 2016-01-27
CA2792234A1 (en) 2011-09-22
CN102939290A (en) 2013-02-20
TWI410423B (en) 2013-10-01
US20110230461A1 (en) 2011-09-22
HUE025774T2 (en) 2016-05-30
JP5496409B2 (en) 2014-05-21
KR20130001276A (en) 2013-01-03
AU2011228699B2 (en) 2016-05-19
CA2792234C (en) 2014-05-27
WO2011114271A8 (en) 2012-11-08
BR112012023664B1 (en) 2020-01-28
KR101455917B1 (en) 2014-11-03
US20140080756A1 (en) 2014-03-20
AR080688A1 (en) 2012-05-02
PH12012501800A1 (en) 2012-12-10
SG183812A1 (en) 2012-10-30
RU2524341C2 (en) 2014-07-27
TW201144312A (en) 2011-12-16
HRP20151232T1 (en) 2015-12-18
JP2013522354A (en) 2013-06-13
ME02330B (en) 2016-06-20
CY1118721T1 (en) 2017-07-12
SI2547679T1 (en) 2015-12-31
DK2547679T3 (en) 2016-01-11
BR112012023664A2 (en) 2016-08-16
HK1182094A1 (en) 2013-11-22

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